Age-Related Increase of Insulin-Degrading Enzyme Is Inversely Correlated with Cognitive Function in APPswe/PS1dE9 Mice

被引:8
作者
Zhang, Yi [1 ]
Wang, Peichang [1 ]
机构
[1] Capital Med Univ, Xuanwu Hosp, Dept Clin Lab, Beijing, Peoples R China
来源
MEDICAL SCIENCE MONITOR | 2018年 / 24卷
基金
中国国家自然科学基金;
关键词
Alzheimer Disease; Amyloid beta; Peptides; Insulysin; Mild Cognitive Impairment; AMYLOID BETA-PROTEIN; ALZHEIMERS-DISEASE; MOUSE MODEL; IN-VIVO; PRECURSOR PROTEIN; APOPTOSIS; PATHOLOGY; DEMENTIA; PLAQUES; PRESENILIN-1;
D O I
10.12659/MSM.909596
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Insulin-degrading enzyme (IDE) is an important regulator for Ab clearance and diabetes. Although it is indispensable in removing plaques related to onset Alzheimer's disease (AD) and in degrading insulin related to diabetes, there have been few studies on the dynamic level of IDE in different stages of AD. Material/Methods: The present study explored the level IDE protein in different stages of APPswe/PS1dE9 mice and their correlations with cognitive decline. The 4-month-old, 10-month-old, and 18-month-old mice were used as the different age stages of mice. Cognitive function was evaluated using the Morris water maze test. We also observed the level of Ab plaques in brain regions of different stages. Results: The data revealed that the expression of IDE was dramatically higher than in age-matched wild mice at the age of 10 months and 18 months. In terms of distribution, Ab plaques were deposited mostly in the cortex and hippocampus, especially in 10-month-old and 18-month-old APPswe/PS1dE9 mice. The cognitive function of 4-month-old APPswe/PS1dE9 mice was not significantly differ in spatial learning. However, the cognitive function, both spatial learning and spatial memory, was dramatically lower in 10-month-old and 18-month-old groups. Conclusions: There was a positive correlation between the expression of IDE and spatial memory in 10-month-old and 18-month-old APPswe/PS1dE9 mice. The study of this protein may provide reference values for the further study of IDE in Alzheimer's disease.
引用
收藏
页码:2446 / 2455
页数:10
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